Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs204999
rs204999
CUI: C0152268
Disease: Nodular Sclerosis Classical Hodgkin Lymphoma
Nodular Sclerosis Classical Hodgkin Lymphoma 		0.810 GeneticVariation GWASDB These SNPs are found on 2 haplotypes associated with NSHL risk (rs204999-rs9268528-rs9268542-rs6903608-rs2858870; AGGCT, OR = 1.7, P = 1.71 × 10(-6); GAATC, OR = 0.4, P = 1.16 × 10(-4)). 22086417

2012
dbSNP: rs204999
rs204999
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 GeneticVariation GWASDB A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. 24920014

2014
dbSNP: rs204999
rs204999
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections 		0.700 GeneticVariation GWASDB A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). 23326239

2013
dbSNP: rs204999
rs204999
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		G 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569

2013
dbSNP: rs204999
rs204999
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 GeneticVariation GWASDB Genome-wide association study of serum albumin:globulin ratio in Korean populations. 23303382

2013
dbSNP: rs204999
rs204999
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		A 0.700 GeneticVariation GWASDB A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. 23936387

2013
dbSNP: rs204999
rs204999
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012
dbSNP: rs204999
rs204999
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		A 0.700 GeneticVariation GWASDB Discovery and fine mapping of serum protein loci through transethnic meta-analysis. 23022100

2012
dbSNP: rs204999
rs204999
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 GeneticVariation GWASDB A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population. 21750111

2011
dbSNP: rs204999
rs204999
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761

2011
dbSNP: rs204999
rs204999
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.700 GeneticVariation GWASDB Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147

2010
dbSNP: rs204999
rs204999
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836

2007
dbSNP: rs204999
rs204999
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007